Epitope mimics for precision immunosuppression
Epitope mimics for precision immunosuppression
批准号:
10075443
负责人:
金额:
$6.25万
依托单位:
依托单位国家:
英国
项目类别:
Grant for R&D
财政年份:
2023
资助国家:
英国
项目状态:
已结题
起止时间:
2023 至 --
中文摘要
Kairos生物技术有限公司旨在改善移植结果和移植等待时间,为以前难以移植的患者。许多终末期器官衰竭的患者体内都有针对潜在供体器官的抗体,这会导致移植排斥反应。这些患者等待移植手术的时间很长,或者可能永远不会接受移植手术。目前的免疫抑制机制倾向于针对整个免疫系统,这可能使患者容易受到感染和癌症等有害副作用的影响。凯洛斯生物技术公司正在设计新的分子“em”,专门针对这些“抗供体”抗体,以及产生这些抗体的细胞。这些分子具有足够的特异性,可以使抗感染抗体保持完整,从而使原本无法进行的移植得以进行。我们目前的研究集中在可用于移植前去除有害抗体或精确靶向产生抗体的细胞的分子上。这种方法有望在移植后用于持续的特异性免疫抑制。预计这些分子也将彻底改变检测和识别特定抗体的方式,从而改善诊断和对抗体介导的排斥反应的理解。第一个应用预计是在诊断测试中检测移植、输血和罕见的自身免疫性疾病中的有害抗体。利用EMs靶向抗供体抗体的相同原理可以应用于自身免疫性疾病的治疗,在这种疾病中,患者循环中的抗体可能会攻击自己的细胞。在自身免疫性疾病中,当抗体攻击患者体内的细胞或攻击移植器官时,EMs将能够特异性抑制这些致病抗体,而不会抑制免疫系统,使患者容易受到感染。
英文摘要
Kairos Biotech Ltd aims to improve transplantation outcomes and transplant waiting times, for previously difficult to transplant patients.Many patients with end-stage organ failure have antibodies to potential donor organs which would cause transplant rejection. These patients wait a long time for a transplant, or may never receive a transplant. Current immunosuppression regimes tend to target the whole immune system which can leave patients vulnerable to deleterious side effects such as infection and cancer.Kairos Biotech are designing novel molecules 'EMs' that specifically target these 'anti-donor' antibodies, and the cells that produce these antibodies. These molecules are specific enough to leave anti-infection antibodies intact thus allowing transplants to proceed that would otherwise not be able to.Our current research focusses on molecules that can be used pre-transplant to either remove deleterious antibodies, or precisely target cells that make the antibodies. This approach is expected to be used post-transplant for continued specific immunosuppression.It is expected that these molecules will also revolutionise the way in which specific antibodies are detected and identified leading to improvements in diagnostics and understandings of antibody-mediated rejection. The first applications are expected to be in diagnostic tests that detect damaging antibodies in transplant, blood transfusion and rare autoimmune diseases.The same principle of using EMs to target anti-donor antibodies can be applied to the treatment of autoimmune diseases where antibodies in the patient's circulation may attack their own cells. In autoimmune conditions where antibodies attack cells in the patient's body or attack transplanted organs the EMs will enable specific suppression of those disease-causing antibodies without supressing the immune system and leaving the patient prone to infection.
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